{"id":257,"date":"2026-07-07T19:23:45","date_gmt":"2026-07-07T17:23:45","guid":{"rendered":"https:\/\/corfoundation.org\/home\/"},"modified":"2026-09-29T18:24:06","modified_gmt":"2026-09-29T16:24:06","slug":"home","status":"publish","type":"page","link":"https:\/\/corfoundation.org\/en\/","title":{"rendered":"Home"},"content":{"rendered":"

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We accelerate scientific breakthroughs to find treatments for neurodevelopmental disorders caused by mutations in the nBAF complex, with a specific focus on the ACTL6B gene. We collaborate closely with patients and families to provide them with the support they need.<\/p>\n

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Become Part of the Breakthrough<\/h2>\n

We unite affected families and science, because without both, it is impossible to find a solution to these challenges. We work around the clock to solve the nBAF complex puzzle by bringing science and families together to move forward in the same direction <\/p>\n

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Transforming hope into clinical results for families worldwide<\/h2>\n

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COR Foundation’s mission is to transform the lives of individuals living with rare neurodevelopmental disorders, providing comprehensive support to them, their families, and caregivers. To achieve this, the organization drives scientific research and access to specialized treatments,<\/strong> promotes awareness and social inclusion, and leverages technology to improve patient monitoring. All of this is made possible through an ongoing network of strategic alliances <\/strong>with the healthcare sector, research centers, public administrations, and non-profit organizations. Bridging the gap between basic genetic research and life-changing therapies. <\/p>\n

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Partners and Supporters<\/h2>\n

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